OBO ID: DOID:12388
Term Name: neurohypophyseal diabetes insipidus Search Ontology:
Synonyms:
  • Pituitary diabetes insipidus
  • vasopressin defective diabetes insipidus
  • Vasopressin deficiency
Definition: A central diabetes insipidus that is characterized by polyuria and polydipsia due to a deficiency in vasopressin synthesis and that has_material_basis_in heterozygous mutation in the arginine vasopressin gene (AVP) on chromosome 20p13. https://pubmed.ncbi.nlm.nih.gov/15070970/
References:
Ontology: Human Disease   ( DOID:12388 )
Relationships
is a type of:
OTHER neurohypophyseal diabetes insipidus PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
AVP Diabetes insipidus, neurohypophyseal 125700
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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